ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Diagnostic Laboratory, Strasbourg University Hospital and "likely pathogenic" from any submitter

Minimum review status of the submission from Diagnostic Laboratory, Strasbourg University Hospital: Collection method of the submission from Diagnostic Laboratory, Strasbourg University Hospital:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_001069.3(TUBB2A):c.872A>C (p.Gln291Pro) rs863224939

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